Canonical Allele Identifier: CA98672301
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1003546222
MyVariant Identifiers: chr4:g.68620105T>A (hg19) chr4:g.67754387T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754387T>A , CM000666.2:g.67754387T>A GRCh38
NC_000004.11:g.68620105T>A , CM000666.1:g.68620105T>A GRCh37
NC_000004.10:g.68302700T>A NCBI36
NG_009293.1:g.6700A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-52A>T MANE Select ENSP00000226413.5:n.-52A>T
NM_000406.2:c.-52A>T NP_000397.1:n.-52A>T
NM_001012763.1:c.-52A>T NP_001012781.1:n.-52A>T
NM_000406.3:c.-52A>T MANE Select NP_000397.1:n.-52A>T
NM_001012763.2:c.-52A>T NP_001012781.1:n.-52A>T
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